Cone rod dystrophy

Definition

A rare genetic isolated inherited retinal disorder characterized by primary cone degeneration with significant secondary rod involvement, with a variable fundus appearance. Typical presentation includes decreased visual acuity, central scotoma, photophobia, color vision alteration, followed by night blindness and loss of peripheral visual field.

Disease data

Classification

Disease

ORPHA code

1872

OMIM code

616502

ICD10 code

H35.5

ICD11 code

9B70

*Soruce